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Astrocytes, Microglia, and Parkinson's Disease

Astrocytes and microglia support well-being and well-function of the brain through diverse functions in both intact and injured brain. For example, astrocytes maintain homeostasis of microenvironment of the brain through up-taking ions and neurotransmitters, and provide growth factors and metabolite...

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Autores principales: Joe, Eun-Hye, Choi, Dong-Joo, An, Jiawei, Eun, Jin-Hwa, Jou, Ilo, Park, Sangmyun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Society for Brain and Neural Science 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5934545/
https://www.ncbi.nlm.nih.gov/pubmed/29731673
http://dx.doi.org/10.5607/en.2018.27.2.77
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author Joe, Eun-Hye
Choi, Dong-Joo
An, Jiawei
Eun, Jin-Hwa
Jou, Ilo
Park, Sangmyun
author_facet Joe, Eun-Hye
Choi, Dong-Joo
An, Jiawei
Eun, Jin-Hwa
Jou, Ilo
Park, Sangmyun
author_sort Joe, Eun-Hye
collection PubMed
description Astrocytes and microglia support well-being and well-function of the brain through diverse functions in both intact and injured brain. For example, astrocytes maintain homeostasis of microenvironment of the brain through up-taking ions and neurotransmitters, and provide growth factors and metabolites for neurons, etc. Microglia keep surveying surroundings, and remove abnormal synapses or respond to injury by isolating injury sites and expressing inflammatory cytokines. Therefore, their loss and/or functional alteration may be directly linked to brain diseases. Since Parkinson's disease (PD)-related genes are expressed in astrocytes and microglia, mutations of these genes may alter the functions of these cells, thereby contributing to disease onset and progression. Here, we review the roles of astrocytes and microglia in intact and injured brain, and discuss how PD genes regulate their functions.
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spelling pubmed-59345452018-05-05 Astrocytes, Microglia, and Parkinson's Disease Joe, Eun-Hye Choi, Dong-Joo An, Jiawei Eun, Jin-Hwa Jou, Ilo Park, Sangmyun Exp Neurobiol Review Article Astrocytes and microglia support well-being and well-function of the brain through diverse functions in both intact and injured brain. For example, astrocytes maintain homeostasis of microenvironment of the brain through up-taking ions and neurotransmitters, and provide growth factors and metabolites for neurons, etc. Microglia keep surveying surroundings, and remove abnormal synapses or respond to injury by isolating injury sites and expressing inflammatory cytokines. Therefore, their loss and/or functional alteration may be directly linked to brain diseases. Since Parkinson's disease (PD)-related genes are expressed in astrocytes and microglia, mutations of these genes may alter the functions of these cells, thereby contributing to disease onset and progression. Here, we review the roles of astrocytes and microglia in intact and injured brain, and discuss how PD genes regulate their functions. The Korean Society for Brain and Neural Science 2018-04 2018-04-24 /pmc/articles/PMC5934545/ /pubmed/29731673 http://dx.doi.org/10.5607/en.2018.27.2.77 Text en Copyright © Experimental Neurobiology 2018. http://creativecommons.org/licenses/by-nc/4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Joe, Eun-Hye
Choi, Dong-Joo
An, Jiawei
Eun, Jin-Hwa
Jou, Ilo
Park, Sangmyun
Astrocytes, Microglia, and Parkinson's Disease
title Astrocytes, Microglia, and Parkinson's Disease
title_full Astrocytes, Microglia, and Parkinson's Disease
title_fullStr Astrocytes, Microglia, and Parkinson's Disease
title_full_unstemmed Astrocytes, Microglia, and Parkinson's Disease
title_short Astrocytes, Microglia, and Parkinson's Disease
title_sort astrocytes, microglia, and parkinson's disease
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5934545/
https://www.ncbi.nlm.nih.gov/pubmed/29731673
http://dx.doi.org/10.5607/en.2018.27.2.77
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